Ananthakrishnan A N, Sakuraba A, Barnes E L, Pekow J, Raffals L, Long M D, Sandler R S
Division of Gastroenterology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.
Inflammatory Bowel Disease Center and Division of Gastroenterology, University of Chicago, Chicago, IL, USA.
Aliment Pharmacol Ther. 2017 Jul;46(2):162-168. doi: 10.1111/apt.14125. Epub 2017 May 3.
The impact of combination therapy on disease-related morbidity in patients with established Crohn's disease (CD) or ulcerative colitis (UC) remains to be well-defined.
To examine the effect of combination therapy on disease outcomes in CD and UC.
Using a multicenter prospective cohort, we classified CD and UC patients as being on monotherapy with anti-TNF or on combination with an immunomodulator. The primary outcome was a composite of new IBD-related surgery, hospitalisations, penetrating complications, need for corticosteroids or new biological at 1 year. Multivariable regression models adjusted for potential confounders.
We included 707 patients with CD (45% combination therapy) and 164 with UC (38% combination therapy). Combination therapy was not associated with reduction in the composite outcome in either CD (OR: 0.87, 95% CI: 0.63-1.22) or UC (OR: 1.45, 95% CI: 0.63-3.38). However, while no difference was noted in those with nonstricturing, nonpenetrating CD, a significant reduction in the likelihood of the outcome was seen in those with stricturing or penetrating CD (30% vs 39%, OR: 0.58, 95% CI: 0.37-0.90). A stronger effect was also observed in those with disease duration <5 years (OR: 0.35, 95% CI: 0.14-0.87) compared to those with a longer duration (OR: 0.75, 95% CI: 0.45-1.27). A similar reduction in occurrence of composite outcome was noted with infliximab and with other anti-TNF biologics.
The benefit of combination immunomodulator-biological therapy is stronger in those with complicated Crohn's disease, particularly early on in their disease course.
联合治疗对已确诊的克罗恩病(CD)或溃疡性结肠炎(UC)患者疾病相关发病率的影响仍有待明确。
研究联合治疗对CD和UC疾病转归的影响。
采用多中心前瞻性队列研究,我们将CD和UC患者分为接受抗TNF单药治疗或联合免疫调节剂治疗。主要结局为1年内新发IBD相关手术、住院、穿透性并发症、使用糖皮质激素或新生物制剂的复合指标。采用多变量回归模型对潜在混杂因素进行校正。
我们纳入了707例CD患者(45%接受联合治疗)和164例UC患者(38%接受联合治疗)。联合治疗与CD(比值比:0.87,95%置信区间:0.63 - 1.22)或UC(比值比:1.45,95%置信区间:0.63 - 3.38)的复合结局降低无关。然而,在非狭窄、非穿透性CD患者中未观察到差异,而在狭窄或穿透性CD患者中结局发生的可能性显著降低(30%对39%,比值比:0.58,95%置信区间:0.37 - 0.90)。与病程较长者(比值比:0.75,95%置信区间:0.45 - 1.27)相比,病程<5年者也观察到更强的效应(比值比:0.35,95%置信区间:0.14 - 0.87)。英夫利昔单抗和其他抗TNF生物制剂在复合结局发生率方面有类似降低。
免疫调节剂 - 生物制剂联合治疗对复杂克罗恩病患者益处更大,尤其是在疾病病程早期。